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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587905Generated: October 26, 2026

1-(2-Methoxyphenyl)piperazine → N-{4-[4-(2-methyloxy-phenyl)piperazinyl]-trans-2-buten-1-yl}phthalimide

https://huagongshe.com/reaction/587905

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
Reactant2-((2E)-4-chlorobut-2-en-1-yl)-2,3-dihydro-1H-isoindole-1,3-dioneHCID 5709374—
ReactantTrans-4-[4-(2-methyloxyphenyl)piperazinyl]-2-buten-1-yl-amineHCID 19917461—
ProductN-{4-[4-(2-methyloxy-phenyl)piperazinyl]-trans-2-buten-1-yl}phthalimideHCID 1146346585.6%

Reaction Steps

Trans-4-[4-(2-methyloxyphenyl)piperazinyl]-2-buten-1-yl-amine: according to the method of Example 5, N-(trans-4-chloro-2-buten-1-yl)phthalimide was reacted with 1-(2-methyloxyphenyl)piperazine to obtain N-{4-[4-(2-methyloxy-phenyl)piperazinyl]-trans-2-buten-1-yl}phthalimide, which was then reacted with hydrazine hydrate. Yield: 85.6%, hydrochloride mp: 178-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227944B2
Source datasetuspto-grants-2016_01
ORD IDord-7a1781fbd38344aa8f6159a37273bc40
Source noteuspto-grants-2016_01